US9175161B2 - Polymer nanocomposite comprising polylactic acid reinforced with the modified phyllosilicate - Google Patents

Polymer nanocomposite comprising polylactic acid reinforced with the modified phyllosilicate Download PDF

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US9175161B2
US9175161B2 US13/814,084 US201113814084A US9175161B2 US 9175161 B2 US9175161 B2 US 9175161B2 US 201113814084 A US201113814084 A US 201113814084A US 9175161 B2 US9175161 B2 US 9175161B2
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phyllosilicate
salt
cation exchange
acetylcholine
trimethyl ammonium
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US20130177723A1 (en
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Susana Aucejo Romero
María Jordá Beneyto
José María Alonso Soriano
Miriam Gallur Blanca
José María Bermúdez Saldaña
Mercedes Hortal Ramos
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Instituto Technologico Del Embalajte Transporte Y Logistica (itene)
INSTITUTO TECNOLOGICO DEL EMBALAJE TRANSPORTE Y LOGISTICA (ITENE)
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Instituto Technologico Del Embalajte Transporte Y Logistica (itene)
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/17—Amines; Quaternary ammonium compounds
    • C08K5/19—Quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00—Use of pretreated ingredients
    • C08K9/04—Ingredients treated with organic substances
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1334—Nonself-supporting tubular film or bag [e.g., pouch, envelope, packet, etc.]
    • Y10T428/1345—Single layer [continuous layer]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/1397—Single layer [continuous layer]

Definitions

  • the present disclosure relates to a polymer nanocomposite containing a modified phyllosilicate, its preparation process, as well as its use for packaging, particularly food packaging.
  • PLA polylactic acid
  • PLA polylactic acid
  • PLA has an insufficient gas barrier property for use as a material for fluid storage containers such as food storage containers.
  • PLA has insufficient mechanical properties in some applications, e.g. packaging, due to its rigidity.
  • PLA has too, insufficient thermal resistance for hot filling or transportation of bottles during the summer months. Hot filling is one of the methods that beverage makers use to reduce the chances pathogens end up in their products. The hot-filling process involves filling containers immediately after the product has been sterilized through a thermal processing operation at high temperature.
  • PLA has limitations in its applications.
  • the incorporation of nano-scale silicate by dispersion in the polymer matrix is a good solution.
  • Nanocomposites are sometimes prepared today using organically modified silicates produced by a cation exchange reaction between the silicate and usually an alkylammonium salt.
  • modified phyllosilicates Preparation of modified phyllosilicates is well known.
  • an organic compound containing a cation that can react by ion exchange with a phyllosilicate containing a negative layer lattice and exchangeable cations does so react to form the modified phyllosilicate.
  • the patent application EP1787918 describes a biodegradable polyester resin reinforced by a phyllosilicate.
  • the phyllosilicate is substituted with ammonium, pyridinium, imidazolium, or phosphonium ions.
  • ammonium ions include tetraethylammonium, octadecyltrimethylammonium, and dimethyldioctadecylammonium among other ions.
  • the resin has improved barrier properties but no consideration is given regarding improvements in the mechanical properties such as the elongation at break.
  • a modified phyllosilicate composition including a hexadecyltrimethyl ammonium cation results in a polymer nanocomposite showing not only improved mechanical properties but also improved barrier properties and thermal resistance.
  • the polymer nanocomposite hereof shows excellent barrier properties is advantageous on the one hand, for its use for storage of aqueous drinks (e.g. water, juice, milk) since the loss of water vapour through the wall of the bottles is minimized.
  • aqueous drinks e.g. water, juice, milk
  • Food containers must present a good barrier property against the diffusion of oxygen into the container, to avoid the spoliation of the food products caused by the presence of oxygen therein.
  • the polymer nanocomposite hereof shows excellent mechanical strength and less rigidity which is an advantage for packaging long term storage, avoiding the polymer nanocomposite deformation and cracking.
  • an aspect of the present disclosure relates to a polymer nanocomposite having a polylactic polymer and a modified phyllosilicate composition, the phyllosilicate having a modifying agent which includes hexadecyl trimethyl ammonium cations which are intercalated between the layers of the phyllosilicate.
  • the silicate used in the nanocomposite hereof belongs to the family of phyllosilicates, preferably smectite group. These compounds are characterized by their swelling properties and high cation-exchange capacities.
  • Different compounds may be added to the polymer nanocomposite, such as pigments, heat stabilizers, antioxidants, water resistant agents, flame retarders, terminal blocking agents, plasticizers, lubricants, mold release agents, antistatic agents, fluorescent brightening agents, processing aids, chain extenders, impact modifiers, UV stabilizers, antifog agents and/or different fillers.
  • processing aids include acrylic polymers.
  • chain extenders include acrylic copolymers.
  • impact modifiers include ethylene, acrylic copolymers and polymers.
  • UV stabilizers include benzotriazol, benzophenones and piperidine derivatives.
  • antioxidants include phenol, phosphates and tocopherol.
  • antistatics include ethoxylated fatty ester.
  • plasticisers include adipates, polyadipates, citrate esters, glycols and polyglycols.
  • antifog agents include ethoxylated fatty ester.
  • Another aspect hereof relates to a process for the preparation of the nanocomposite as defined above, which includes the following operations: a) drying the modified phyllosilicate and the polylactic polymer, and b) melt-blending the biodegradable polymer and the modified phyllosillicate by an extruder.
  • the improved mechanical, thermal and barrier properties of the polymer nanocomposite make it especially useful as a container, bag or film.
  • Another aspect of the present disclosure relates to a container, bag or film made of the nanocomposite as defined above.
  • FIG. 1 shows the young Modulus (GPa), (white column) and the elongation at break (mm), (black column) of different samples.
  • FIG. 2 shows the young Modulus (GPa), (white column) and the elongation at break (mm), (black column) of different samples.
  • FIG. 3 shows a plot of the heat flow versus temperature of different samples.
  • an aspect of the present disclosure relates to a polymer nanocomposite including a polylactic polymer and a modified phyllosilicate composition.
  • polymer nanocomposite refers to a polymeric material and a reinforcing nanoscale material.
  • the nanoscale material has at least one dimension in the nanometer size range.
  • the reinforcing nanoscale material is the modified phyllosilicate composition of the present disclosure with a lamellae thickness around 1 nm.
  • phyllosilicates refers to layered silicates in which the SiO 4 tetrahedra are linked together in two dimensional sheets and are condensed with layers of AlO 6 or MgO octahedra in the ratio 2:1 or 1:1.
  • the negatively charged layers attract positive cations (e.g. Na + , K + , Ca 2+ , Mg 2+ .) which can hold the layers together.
  • Non-limiting exemplar phyllosilicates which may be used within the scope hereof are sodium montmorillonite, magnesium montmorillonite, calcium montmorillonite. In a preferred implementation, the phyllosilicate is sodium montmorillonite.
  • modified phyllosilicates refers to phyllosilicates wherein the positive cations (e.g. Na + , K + , Ca 2+ , Mg 2+ ), are exchanged by ion exchange reactions with alkylammonium cations as modifying agents.
  • the modified phyllosilicate hereof includes hexadecyl trimethyl ammonium and, optionally acetylcholine or choline cations, as modifying agents.
  • PLA polylactic
  • PLA refers to a biodegradable, thermoplastic, aliphatic polyester derived from renewable sources.
  • PLA includes poly-L-lactide (PLLA), the product resulting from polymerization of L,L-lactide and poly-D-lactide (PDLA), the product resulting from polymerization of D,L-lactide. All commercial grades are included in the term PLA as used herein, commercial grades are copolymers of PLLA and PDLA in different ratios.
  • the ratio phyllosilicate composition/polylactic polymer is between about 0.5:99.5 and about 20:80 weight/weight ratio. In a more preferred implementation the ratio phyllosilicate composition/polylactic polymer is between about 2:98 and about 18:82 weight/weight ratio. In another more preferred implementation the ratio phyllosilicate composition/polylactic polymer is between about 4:96 and about 16:84 weight/weight ratio.
  • the modifiers are added in excess to the cation exchange capacity (CEC) of the phyllosilicate and a value of 0.5-10 times the CEC was established as the optimum.
  • CEC cation exchange capacity
  • the amount of acetylcholine or choline is 0.20-0.75 meq/100 g the value of the phyllosilicate CEC and the amount of hexadecyl trimethyl ammonium cation is 5.25-5.80 meq/100 g the value of the phyllosilicate CEC.
  • the amount of acetylcholine or choline is 0.25-0.50 meq/100 g the value of the phyllosilicate CEC and the amount of hexadecyl trimethyl ammonium cation is 5.55-5.75 meq/100 g the value of the phyllosilicate CEC.
  • the corresponding nanocomposite can be obtained by a process which includes the following operations: a) drying the modified phyllosilicate and the polymer, and b) melt-blending the biodegradable polymer and the modified phyllosillicate with an extruder.
  • melt-blending operation is carried out at a temperature between 190° C.-210° C.
  • the process further includes a previous operation of preparing the modified phyllosilicate which includes the operations: (a) dispersing the phyllosillicate in water and an C 1 -C 10 alcohol; (b) applying an ultrasonic wave; (c) optionally adding choline salt or acetylcholine salt (d) adding hexadecyl trimethyl ammonium salt; (e) maintaining the mixture of operation (d) at a temperature comprised between 20° C. and 120° C.; (f) isolating the compound obtained in operation (d), wherein the operations a), b), c), and d) can be carried out in any order.
  • a previous operation of preparing the modified phyllosilicate which includes the operations: (a) dispersing the phyllosillicate in water and an C 1 -C 10 alcohol; (b) applying an ultrasonic wave; (c) optionally adding choline salt or acetylcholine salt (d) adding hexadecyl tri
  • the phyllosilicate is dispersed in water and ethanol.
  • the choline salt added is choline halide. In a more preferred implementation the choline salt added is choline chloride.
  • the acetylcholine salt added is acetylcholine halide. In a more preferred implementation the acetylcholine salt added is acetylcholine chloride.
  • the hexadecyl trimethyl ammonium salt added is hexadecyl trimethyl ammonium halide. In a more preferred implementation the hexadecyl trimethyl ammonium salt added is hexadecyl trimethyl ammonium bromide.
  • choline salt or acetylcholine salt and the addition of hexadecyl trimethyl ammonium salt is carried out slowly.
  • the mixture of operation (d) is maintained at a temperature between about 20° C. and about 90° C. In another preferred implementation, the mixture of operation (d) is maintained at a temperature between about 50° C. and about 90° C. In a more preferred implementation the mixture of operation (d) is maintained at a temperature between about 65° C. and about 75° C.
  • the isolating operation includes purifying of the prepared modified phyllosilicate.
  • the phyllosilicate is purified with a solution of water:ethanol, in particular, the solution is added to the modified phyllosilicate, and the mixture is maintained under stirring at a temperature between about 50° C. to about 90° C.
  • the product is filtered and the conductivity of the mother liqueours is measured. This process is repeated until the mother liqueours have a conductivity below 5-30 ⁇ S/cm.
  • the isolating operation includes a drying operation of the phyllosilicate after the purification.
  • the drying operation is carried out at a temperature between about 70° C. and about 90° C. It can be carried out in a conventional oven, by lyophilisation or by atomization. Generally, the drying process lasts at least about 12 hours.
  • the phyllosilicate can be milled, and sieved. Generally it is sieved to a particle size below 25 microns.
  • Purified sodium montmorillonite (Closiste® Na + ) was purchased from Southern Clay Products, with moisture content between 4 and 9%. CEC of sodium montmorillonite was 92.6 mequiv/100 g.
  • Quaternary ammonium salts were supplied by Acros Organics. Choline (CO) chloride, acetylcholine (ACO) chloride, and hexadecyltrimethyl ammonium (HDTA) bromide with 99% of purity, and trimethyloctadecylammonium bromide 98% were purchased from Fluka.
  • the next operation includes purifying the prepared modified phyllosilicate.
  • a 11 solution 50:50 vol water:ethanol was prepared. After filtering the mixture under vacuum, fresh solution was added to the modified phyllosilicate, and the mixture was maintained under stirring at 70° C. at least 2 hours. The procedure was repeated until the solution filtered was below 5 ⁇ S/cm in conductivity.
  • the next operation includes drying of the phyllosilicate at 70° C. during at least 12 hours. Finally, the phyllosilicate was milled, and sieved to a particle size below 25 microns.
  • the modified phyllosilicate obtained is a Cloisite (CLO) with 5.5 CEC of HDTA and 0.5 CEC of ACO.
  • a CLO with 5.75 CEC of HDTA and 0.25 CEC of ACO was obtained following the process of Example 1b but using the ACO halide dissolved in 250 ml of ethanol.
  • ACO mass was 0.84 grams, and HDTA mass was 38.81 grams.
  • Example 2 For the production of the montmorillonite modified with hexadecyltrimethyl ammonium cations, the same process of Example 1 was carried out but starting from 40.50 grams of hexadecyltrimethyl ammonium bromide which has been dissolved in 500 ml of ethanol.
  • the modified phyllosilicate obtained is a CLO with 6 CEC of HDTA.
  • PLA4042-Phyllosilicate (Montmorillonite with 5.5 CEC of HDTA and 0.5 CEC of ACO)
  • PLA nanocomposite samples were obtained with the modified phyllosilicate prepared in Example 1a, and PLA 4042.
  • a DSM Xplore Microcompounder 15 cc was used. PLA pellets (dried overnight at 60° C.) were blended with 4% by weight of modified phyllosilicate in this co-rotating twin screw micro-extruder. The temperature of processing was 200° C. The rotation speed of the screw was maintained at 100 r.p.m., and residence time was set to 10 min. After extrusion, the melted materials were transferred through a preheated cylinder (200° C.) to the mini injection moulding machine (4 cc) (DSM Xplore) to obtain bone-like specimen samples (ISO 527 standard; probe type 5A-B)
  • PLA4042-Phyllosilicate (Montmorillonite with 5.75 CEC of HDTA and 0.25 CEC of ACO)
  • Example 3a The same process of Example 3a was carried out but with the modified phyllosilicate prepared in Example 1b.
  • PLA4042-Phyllosilicate (Montmorillonite with 5.75 CEC of HDTA and 0.25 CEC of CO)
  • Example 3a The same process of Example 3a was carried out but with the modified phyllosilicate prepared in Example 1c.
  • Example 3a The same process of Example 3a was carried out but with the modified phyllosilicate prepared in Example 2.
  • PLA2002-Phyllosilicate (Montmorillonite with 5.75 CEC of HDTA and 0.25 CEC of ACO)
  • Example 3a The same process of Example 3a was carried out but with PLA2002 and the modified phyllosilicate prepared in Example 1b.
  • Example 3a The same process of Example 3a was carried out but with PLA2002 and the modified phyllosilicate prepared in Example 2.
  • Example 3a The same process of Example 3a was carried out but with the modified phyllosilicates prepared in Comparative example 1.
  • Example 3a The same process of Example 3a was carried out but with PLA2002 and with the modified phyllosilicates prepared in Comparative example 1.
  • Results are presented in FIG. 1 showing the Young Modulus and the elongation at break of PLA, (nanocomposites obtained in Example 3a, 3b, and 3c).
  • the Young Modulus was increased in the case of PLA nanocomposite versus PLA pure, and also an increase in the elongation at break was observed (best result obtained with nanocomposites prepared in Example 3b) with respect to PLA pure. This was an unexpected result since an increase in Young Modulus generally implies a decrease in the elongation at break.
  • Comparative results of nanocomposites based on PLA 4042 are shown in FIG. 2 . It can be seen that the use of modified phyllosilicate of the present disclosure produces an increase in Young Modulus, and also an increase in the elongation at break, as occurred previously in respect of the nanocomposite of comparative example 2. Elongation at break reaches higher values when nanocomposites prepared in Example 3f and 3b were used.
  • Results are shown in Table 1. The smaller the value of the water vapour permeability, the more excellent is the barrier property.
  • nanocomposites hereof show a higher reduction of WVTR than the closest prior phyllosilicates. Best results were reached with the nanocomposite prepared in Example 3d, with an improvement of 74%.
  • the nanocomposites hereof show a high reduction of WVTR when the phyllosilicates is added. This reduction is higher than pure PLA and the reduction showed by the closest prior phyllosilicate (comparative example 3). Best results were reached with the nanocomposite prepared in Example 3f, with an improvement of 67%.
  • Oxygen transmission rate was evaluated following standard ASTM D3985: “Standard Test Method for Oxygen Gas Transmission Rate Through Plastic Film and Sheeting Using a Coulometric Sensor”. Experimental equipment was an OX-TRAN 2/20 SM. The measurements conditions were 23° C. and 50% relative humidity. The test was performed with oxygen (100%).
  • a differential scanning calorimetric technique was used to show what happens to the different nanocomposites (Ex. 3a, 3b, 3d and Comparative Ex. 2) and PLA 4042 when the nanocomposites and polymer reach melting temperature.
  • nanocomposites of the present disclosure had a melting point higher than PLA.
  • the nanocomposites of the present disclosure have similar to (Ex. 3d) or better than (Ex. 3a) the thermal properties of the nanocomposite with octadecyltrimethylammonium.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Wrappers (AREA)
  • Biological Depolymerization Polymers (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Packging For Living Organisms, Food Or Medicinal Products That Are Sensitive To Environmental Conditiond (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
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EP10382216.9 2010-08-04
EP10382216 2010-08-04
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PCT/EP2011/063405 WO2012017025A1 (en) 2010-08-04 2011-08-03 Polymer nanocomposite comprising polylactic acid reinforced with the modified phyllosilicate

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US11912926B2 (en) 2018-09-04 2024-02-27 Saudi Arabian Oil Company Synthetic functionalized additives, methods of synthesizing, and methods of use

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* Cited by examiner, † Cited by third party
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ES2534842T3 (es) * 2010-08-04 2015-04-29 Instituto Tecnológico Del Embalaje, Transporte Y Logística Itene Filosilicato modificado
JP5889671B2 (ja) * 2012-02-24 2016-03-22 旭化成ケミカルズ株式会社 エチレン酢酸ビニル共重合体樹脂組成物
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EP3166719B1 (en) * 2014-07-11 2022-11-09 Elementis Specialties, Inc. Organoclay compositions having quaternary ammonium ion having one or more branched alkyl substituents
US9562145B2 (en) 2014-07-11 2017-02-07 Elementis Specialties, Inc. Organoclay compositions having quaternary ammonium ion having one or more branched alkyl substituents
JP6398406B2 (ja) * 2014-07-15 2018-10-03 富士ゼロックス株式会社 ポリ乳酸樹脂変性用の改質剤、樹脂組成物及び樹脂成形体
JP6704915B2 (ja) * 2014-12-09 2020-06-03 スマートポリマー、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツングＳｍａｒｔｐｏｌｙｍｅｒ Ｇｍｂｈ 対象の活性成分の放出を行う成形機能性セルロース物品の製造方法
CN105199347B (zh) * 2015-10-09 2017-10-13 湖北工业大学 Pla/mmt降解增强母料共混改性pla/pbat复合材料及其制备方法
BR112019004049B1 (pt) 2016-09-15 2023-01-10 Instituto Tecnológico Del Embalaje, Transporte Y Logística (Itene) Nanocompósito polimérico compreendendo poli(tereftalato de etileno) reforçado com um filossilicato intercalado
CN107099116A (zh) * 2017-05-18 2017-08-29 湖南省达琪新材料有限公司 聚酰胺多胺插层层状硅酸盐复合材料的制备方法
CN108821301B (zh) * 2018-06-08 2022-06-21 安徽艾米伦特建材科技有限公司 保温材料用改性蒙脱土及其制备方法
CN109796646A (zh) * 2018-12-12 2019-05-24 青岛大学 一种碳纳米管改性层状硅酸盐协同增强充油型多元溶液共凝橡胶及其制备方法
WO2020219447A1 (en) 2019-04-23 2020-10-29 Elementis Specialties, Inc. Slurry compositions containing mixed branched alkyl organoclay compositions

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2771308A1 (fr) 1997-11-25 1999-05-28 Inst Francais Du Petrole Procede d'isomerisation des normales paraffines c5-c10 utilisant un phyllosilicate 2:1 dioctaedrique ponte a grande distance reticulaire
US20040042750A1 (en) * 2002-08-09 2004-03-04 Gillberg Gunilla E. Clay nanocomposite optical fiber coating
EP1787918A1 (en) 2004-06-10 2007-05-23 Unitika, Ltd. Biodegradable gas barrier vessel and process for producing the same
WO2009127000A1 (en) * 2008-04-15 2009-10-22 The University Of Queensland Polymer composites having particles with mixed organic modifications

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6379773A (ja) * 1986-09-19 1988-04-09 松下電工株式会社 無機層状多孔体の製法
JPS6385067A (ja) * 1986-09-25 1988-04-15 松下電工株式会社 無機層状多孔体の製法
BR9707663A (pt) * 1996-02-23 1999-04-13 Dow Chemical Co Compósito de polímero
CZ273598A3 (cs) * 1996-12-31 1999-01-13 The Dow Chemical Company Kompozity polymer-organické jíly a jejich příprava
JPH11131047A (ja) * 1997-10-29 1999-05-18 Co-Op Chem Co Ltd 有機−粘土複合体と有機溶剤よりなる組成物
TWI254063B (en) * 2000-05-09 2006-05-01 Ind Tech Res Inst sPS nanocomposites and processes for producing the same
JP2001316516A (ja) * 2000-05-11 2001-11-16 Yazaki Corp 架橋シリコーンゴム廃棄物の再生方法
JP2002338796A (ja) * 2001-05-21 2002-11-27 Teijin Ltd 生分解性ガスバリア材料
CN1182190C (zh) * 2001-09-27 2004-12-29 中国科学院长春应用化学研究所 原位聚合制备聚烯烃/无机组份纳米复合材料的方法
JP2006347787A (ja) * 2005-06-13 2006-12-28 Fujifilm Holdings Corp 有機変性層状珪酸塩及びポリエステル樹脂組成物
ES2277563B1 (es) * 2005-12-29 2008-06-16 Nanobiomatters, S.L. Procedimiento de fabricacion de materiales nanocompuestos para aplicaciones multisectoriales.
US7928154B2 (en) * 2006-06-26 2011-04-19 Sabic Innovative Plastics Ip B.V. Methods of preparing polymer-organoclay composites and articles derived therefrom
JP2008075068A (ja) * 2006-08-25 2008-04-03 Canon Inc 樹脂組成物
JP5146868B2 (ja) * 2006-09-06 2013-02-20 独立行政法人物質・材料研究機構 ポリ乳酸複合材料
US20090018264A1 (en) * 2007-07-12 2009-01-15 Canon Kabushiki Kaisha Resin composition
JP2009242775A (ja) * 2008-03-13 2009-10-22 Toray Ind Inc 難燃性ポリエステル樹脂組成物およびそれからなる繊維構造物
ES2534842T3 (es) * 2010-08-04 2015-04-29 Instituto Tecnológico Del Embalaje, Transporte Y Logística Itene Filosilicato modificado

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2771308A1 (fr) 1997-11-25 1999-05-28 Inst Francais Du Petrole Procede d'isomerisation des normales paraffines c5-c10 utilisant un phyllosilicate 2:1 dioctaedrique ponte a grande distance reticulaire
US6191333B1 (en) 1997-11-25 2001-02-20 Institut Francais Du Petrole Process for isomerization of normal C5-C10 paraffins using bridged long-reticulate-distance dioctahedral phyllosilicate 2:1
US20040042750A1 (en) * 2002-08-09 2004-03-04 Gillberg Gunilla E. Clay nanocomposite optical fiber coating
EP1787918A1 (en) 2004-06-10 2007-05-23 Unitika, Ltd. Biodegradable gas barrier vessel and process for producing the same
WO2009127000A1 (en) * 2008-04-15 2009-10-22 The University Of Queensland Polymer composites having particles with mixed organic modifications

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
ASTM Designation D: 3985-02, Standard Test Method for Oxygen Gas Transmission Rate Through Plastic Film and Sheeting Using a Coulometric Sensor, ASTM International, (the year of publication is sufficiently earlier than the effective U.S. filing date and any foreign priority date so that the particular month of publication is not in issue) 2002, pp. 1-6, ASTM International, West Conshohocken, PA, USA.
ASTM E96: Standard Test Methods for Water Vapor Transmission of Materials, 24 CFR 3880.504(a), American Society for Testing and Materials, (the year of publication is sufficiently earlier than the effective U.S. filing date and any foreign priority date so that the particular month of publication is not in issue) 1995, pp. 785-792, American Society for Testing and Materials, Philadelphia, PA, USA.
Aucejo-Romero et al., Approved clay-biopolymer nanocomposites for food contact applications, 16th IAPRI World Conference on Packaging Book of Abstracts, p. 81, Jun. 8-12, 2008, Bangkok, Thailand.
British Standard Institute, BS EN ISO 527-1:1996, BS 2782-3: Method 321:1994, ISO 527-1:1993, Incorporating Amendment No. 1, Plastics-Determination of tensile properties, (the year of publication is sufficiently earlier than the effective U.S. filing date and any foreign priority date so that the particular month of publication is not in issue) 1996, pp. 1-16, British Standard Institute, London, England. English language counterpart to EN ISO 527-1 cited above.
European Standard, EN ISO 527-1, Version En espanol, Plasticos Determinacion de las propiedades en traction, Parte 1: Principios Generales, (ISO 527-1:1993 incluye Corr 1:1994), Feb.,1996, pp. 1, 4-16, CEN, Comite Europeo De Normalizacion, European Committee for Standardization, Comite Europeen de Normalisation, Europaisches Komitee fur Normung, Bruxelles, Belgium. English language counterpart is BS EN ISO 527-1 cited below.
International Search Report and Written Opinion of the International Searching Authority, Search Report, Application No. PCT/EP2011/063405 issued by the European Patent Office, Munich, Germany, dated Sep. 14, 2011.
PLA 2002D Data Sheet. 2005. *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11332651B2 (en) 2018-09-04 2022-05-17 Saudi Arabian Oil Company Synthetic functionalized additives, methods of synthesizing, and methods of use
US11912926B2 (en) 2018-09-04 2024-02-27 Saudi Arabian Oil Company Synthetic functionalized additives, methods of synthesizing, and methods of use
WO2020056087A1 (en) * 2018-09-13 2020-03-19 Saudi Arabian Oil Company Charged composite materials, methods of synthesizing, and methods of use
US11242478B2 (en) 2018-09-13 2022-02-08 Saudi Arabian Oil Company Charged composite materials, methods of synthesizing, and methods of use

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